| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268287 | Tetrahedron Letters | 2015 | 4 Pages |
Abstract
Vinyl sulfones and vinyl sulfone-modified carbohydrates were subjected to 1,3-dipolar-cycloaddition reactions with four different azidofuranosides having azido groups at the C5 and C6-positions under refluxing conditions in aqueous media without any metal catalyst to afford the 1,5-disubstituted 1,2,3-triazolylated monofuranosides and difuranosides in high yields. These syntheses of 1,5-disubstituted triazolylated monosaccharides as well as 1,5-disubstituted 1,2,3-triazole linked disaccharides open up a new possibility of connecting furanosides with a stable-triazole backbone.Download high-res image (55KB)Download full-size image
Graphical abstractDownload high-res image (130KB)Download full-size image
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anirban Kayet, Santu Dey, Tanmaya Pathak,